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IDELVION: A Comprehensive Review of Clinical Trial and Real-World Data

Hemophilia B is a bleeding disorder caused by a deficiency of coagulation factor IX (FIX). Treatment with FIX replacement products can increase FIX activity levels to minimize or prevent bleeding events. However, frequent dosing with standard-acting FIX products can create a high treatment burden. L...

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Autores principales: Escobar, Miguel, Mancuso, Maria Elisa, Hermans, Cedric, Leissinger, Cindy, Seifert, Wilfried, Li, Yanyan, McKeand, William, Oldenburg, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875492/
https://www.ncbi.nlm.nih.gov/pubmed/35207344
http://dx.doi.org/10.3390/jcm11041071
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author Escobar, Miguel
Mancuso, Maria Elisa
Hermans, Cedric
Leissinger, Cindy
Seifert, Wilfried
Li, Yanyan
McKeand, William
Oldenburg, Johannes
author_facet Escobar, Miguel
Mancuso, Maria Elisa
Hermans, Cedric
Leissinger, Cindy
Seifert, Wilfried
Li, Yanyan
McKeand, William
Oldenburg, Johannes
author_sort Escobar, Miguel
collection PubMed
description Hemophilia B is a bleeding disorder caused by a deficiency of coagulation factor IX (FIX). Treatment with FIX replacement products can increase FIX activity levels to minimize or prevent bleeding events. However, frequent dosing with standard-acting FIX products can create a high treatment burden. Long-acting products have been developed to maintain bleed protection with extended dosing intervals. Recombinant factor IX–albumin fusion protein (rIX-FP) is a long-acting product indicated for the treatment and prophylaxis of bleeding events and perioperative management in adult and pediatric patients. This review outlines data from all previously treated patients in the Prophylaxis and On-Demand Treatment using Longer Half-Life rIX-FP (PROLONG-9FP) clinical trial program and summarizes real-world data evaluating the use of rIX-FP in routine clinical practice. In the PROLONG-9FP program, rIX-FP demonstrated effective hemostasis in all patients at dose regimens of up to 21 days in patients aged ≥ 18 years and up to 14 days in patients aged < 12 years. rIX-FP has a favorable pharmacokinetic profile and an excellent safety and tolerability profile. Extended dosing intervals with rIX-FP led to high levels of adherence and reduced consumption compared with other FIX therapies. Data from real-world practice are encouraging and reflect the results of the clinical trials.
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spelling pubmed-88754922022-02-26 IDELVION: A Comprehensive Review of Clinical Trial and Real-World Data Escobar, Miguel Mancuso, Maria Elisa Hermans, Cedric Leissinger, Cindy Seifert, Wilfried Li, Yanyan McKeand, William Oldenburg, Johannes J Clin Med Review Hemophilia B is a bleeding disorder caused by a deficiency of coagulation factor IX (FIX). Treatment with FIX replacement products can increase FIX activity levels to minimize or prevent bleeding events. However, frequent dosing with standard-acting FIX products can create a high treatment burden. Long-acting products have been developed to maintain bleed protection with extended dosing intervals. Recombinant factor IX–albumin fusion protein (rIX-FP) is a long-acting product indicated for the treatment and prophylaxis of bleeding events and perioperative management in adult and pediatric patients. This review outlines data from all previously treated patients in the Prophylaxis and On-Demand Treatment using Longer Half-Life rIX-FP (PROLONG-9FP) clinical trial program and summarizes real-world data evaluating the use of rIX-FP in routine clinical practice. In the PROLONG-9FP program, rIX-FP demonstrated effective hemostasis in all patients at dose regimens of up to 21 days in patients aged ≥ 18 years and up to 14 days in patients aged < 12 years. rIX-FP has a favorable pharmacokinetic profile and an excellent safety and tolerability profile. Extended dosing intervals with rIX-FP led to high levels of adherence and reduced consumption compared with other FIX therapies. Data from real-world practice are encouraging and reflect the results of the clinical trials. MDPI 2022-02-18 /pmc/articles/PMC8875492/ /pubmed/35207344 http://dx.doi.org/10.3390/jcm11041071 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Escobar, Miguel
Mancuso, Maria Elisa
Hermans, Cedric
Leissinger, Cindy
Seifert, Wilfried
Li, Yanyan
McKeand, William
Oldenburg, Johannes
IDELVION: A Comprehensive Review of Clinical Trial and Real-World Data
title IDELVION: A Comprehensive Review of Clinical Trial and Real-World Data
title_full IDELVION: A Comprehensive Review of Clinical Trial and Real-World Data
title_fullStr IDELVION: A Comprehensive Review of Clinical Trial and Real-World Data
title_full_unstemmed IDELVION: A Comprehensive Review of Clinical Trial and Real-World Data
title_short IDELVION: A Comprehensive Review of Clinical Trial and Real-World Data
title_sort idelvion: a comprehensive review of clinical trial and real-world data
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875492/
https://www.ncbi.nlm.nih.gov/pubmed/35207344
http://dx.doi.org/10.3390/jcm11041071
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